Efficacy of Best Possible Self Intervention Over Time

December 19, 2014 updated by: Universitat Jaume I

Efficacy of Best Possible Self Intervention Over Time: A Randomized Control Trial

This study is aimed to test the efficacy of a Positive Psychology Intervention (Best Possible Self) over optimism, future expectancies and positive affect at mid-term, in comparison to a control group. The principal hypothesis is that Best Possible Self intervention will enhance significantly the levels of optimism and positive affect in comparison to the control group at short and mid-term.

Study Overview

Detailed Description

Over the last fifteen years, research in the field of positive psychology has increased exponentially (Bolier, Haverman, Westerhof, Riper, Smit & Bohlmeijer, 2013; Sin & Lyubomirsky, 2009). These studies have shown that positive moods and positive emotions lead people to think, feel, and act in favor of their approach goals, promoting their involvement in them (Lyubomirsky, 2001). One of the main arms of this framework, is the development of exercises and treatment protocols aimed to promote the appearance of different positive emotions and states, called Positive Psychology Interventions (PPIs).

In this sense, Best Possible Self (BPS) has been included as a PPI, since is aimed to enhance wellbeing. Specifically, BPS is a positive future thinking technique, which requires people to envision themselves in the future, after everything has gone as good as it possibly could. This exercise has shown efficacy improving optimism, future expectancies and positive affect compared to a control condition, in general population (Meevissen, Peters & Alberts, 2011; Sheldon &Lyubomirsky, 2012; Peters, Flink, Boersma & Linton, 2010).

Furthermore, the progress of Information and Communication Technologies (ICTs), has allowed the development of technology applications and devices that could enhance the quality of experience and the wellbeing levels. This approach is called Positive Technology (PT) and it can be used as a complement to PPIs. PT can be defined as the scientific and applied approach to improve the quality of our personal experience trying to increase wellness and generate strengths (Riva, Baños, Botella, Wiederhold & Gaggioli, 2012).

Taking into account the prior literature, the aim of the present study is to carry out a randomized controlled study in order to replicate the findings about the effects of BPS on optimism, mood and affect in young general population. The exercise will be applied through a Positive Technology system and the effects will be analyzed during four months. The design employed in this study is similar to the used in other studies (Meevissen et al, 2011; Renner, Schwarz, Peters & Huibers, 2014; Sheldon & Lyubomirsky, 2006).

Study Type

Interventional

Enrollment (Actual)

78

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Castellón, Spain, 12006
        • University Jaume I

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Be between 18 and 70 years old.
  • Be willing to participate in the study.
  • Have an e-mail address.

Exclusion Criteria:

  • Presence of severe physical illness.
  • Presence of psychological disorders.
  • Be receiving psychological treatment.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: BPS exercise
Intervention group which requires people to envision themselves in a future in which all has gone in the best possible way.

Participants are asked to write and imagine about a future in which they have reached all their goals and they have developed all their potentialities in four different domains: personal, professional, social and health domain.

They carry out the exercise in a Positive Technology System called the "Book of Life", which has shown efficacy in the enhancement of positive mood (Baños, Etchemendy, Farfallini, García-Palacios, Quero & Botella, 2014). This application looks like a personal diary, where participants can write all that they want and these essays are supported by multimedia content (pictures, songs and videos). Additionally, they can continue doing the exercise in a web platform in which they can visualize all the content they had developed previously.

Other Names:
  • Best Possible Self
  • Positive Psychology Intervention
Placebo Comparator: Daily Activities
Control group which consists of thinking and writing about all the activities and situations that had taken place during the last 24 h.
Participants are asked to think and write about all that they have done the last 24 hours. They carry out the exercise in a powerpoint document, where they can record all the activities, situations and thoughts.
Other Names:
  • Best Possible Self
  • Positive Psychology Intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Subjective Probability Task (SPT; MacLeod, 1996).
Time Frame: 4 months
This scale measures positive and negative expectancies about future events. It consists of 20 statements referring to negative expectancies and 10 statements referring to positive expectancies. Participants answer on a 7-point scale (Not at all likely to occur - Extremely likely to occur). Some studies have found an appropriate levels of internal consistency for positive and negative expectancies (α=0.80-0.82 y 0.91, respectively).
4 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Positive and Negative Affect Scale (PANAS, Watson, Clark & Tellegen, 1988; Sandín et al., 1999).
Time Frame: 4 months
This measure analyzes the levels of positive (PA) and negative affect (NA). The instrument consists of 20 items, 10 for each level of affect. Participants rate on a 5-point scale (Not at all - Extremely). The Spanish version has demonstrated high internal consistency (0.89 to 0.91 for PA and NA in women and 0.87 for AP and 0.89 for AN in men) in college students.
4 months
Life Orientation Test (Lot-R; Otero, Luengo, Romero Gómez & Castro, 1998; Scheier, Carver & Bridges, 1994).
Time Frame: 4 months
This scale measures positive and negative expectancies about future events. It consists of 20 statements referring to negative expectancies and 10 statements referring to positive expectancies. Participants answer on a 7-point scale (Not at all likely to occur - Extremely likely to occur). Some studies have found an appropriate levels of internal consistency for positive and negative expectancies (α=0.80-0.82 y 0.91, respectively).
4 months
Beck Depression Inventory II (BDI-II; Beck, 1996)
Time Frame: 4 months
This is one of the most widely questionnaires used to evaluate severity of depression in pharmacological and psychotherapy trials. The instrument has good internal consistency (Cronbach's alpha of 0.76 to 0.95) and test-retest reliability of around 0.8. The Spanish version of this instrument has also shown a high internal consistency (Cronbach's alpha of 0.87) for both the general and the clinical population (Cronbach's alpha of 0.89). Summed to obtain the total score, which can be a maximum of 63 points.
4 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Eysenck Personality Questionnaire - Revised - Neuroticism (EPQ-R-N; Eysenck, Eysenck & Barrett, 1985; Eysenck & Eysenck, 1997).
Time Frame: Baseline
This scale assesses the neuroticism level of the individual, showing if he is stable or neurotic. This subscale is composed by 12 items of dicotomic response (yes-not). Regarding psychometric properties, Eysenck and Eysenck (1997) got an alpha coefficient between 0-73 and 0.82.
Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Cristina Botella, Professor, Universitat Jaume I
  • Study Director: Juana M Bretón, Assistant Professor, Universitat Jaume I
  • Study Chair: Angel Enrique, PhD student, Universitat Jaume I

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2013

Primary Completion (Actual)

August 1, 2014

Study Completion (Actual)

October 1, 2014

Study Registration Dates

First Submitted

December 17, 2014

First Submitted That Met QC Criteria

December 19, 2014

First Posted (Estimate)

December 22, 2014

Study Record Updates

Last Update Posted (Estimate)

December 22, 2014

Last Update Submitted That Met QC Criteria

December 19, 2014

Last Verified

December 1, 2014

More Information

Terms related to this study

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